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Microbial Pathogenesis

How do bacteria cause disease ?

1- Direct toxic effects – proteases – flesh eating bacteria

2- Activation of the host immune system –Local – inflammation – PUSSystemic – cardiovascular effects - SEPSIS

Bacterial activation of the host immune response

Subclinical Symptomatic

Innate/AcquiredClearance mechanisms

“Appropriate” Excessive

Septic ShockDeath

Resolution

E. coli - Eosin-methylene blue plateE.coli - lining up forlunch….

How do E.coli become pathogens ?

Commensal flora –

Acquire genes that cause disease –

Colonization – attachment

Toxin of some sort –

E. Coli – UTI’s - urinary tract infection – activate a PMN response

Diarrheal disease – interact with gut epithelial cells –cause fluid secretion

Sepsis – get into the blood – activate immune cells

Prototypic E.coli

avirulent in gut - commensalflora

Genomic DNA

Sex pilus

Flagella

Prototypic E.coli

Genomic DNA + pathogenicityisland (phage DNA)

Plasmid DNA- encoding pili;toxins, single organismcan express > 1 type ofpilus

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Urinary tract infection : Adherence

Fecal contamination of the bladder, urethra (primarily in females)Acquire a new organism from a partner

Organisms which express pili which bind to CHO

receptors on the uroepithelial cell - Gal-Gal - dissacharideligand - Genetic susceptibility- display the receptor - acquire the organism which expresses the type1 pilus

Ligand - Receptor interaction

Activates epithelial pro-inflammatoryresponse

IL-8 - PMN chemokine

PMN’s

Toxic products

Reactive oxygen intermediatesSuperoxideNeutrophil elastase

PMN mediated damage

Adherence UTIICAM, CD11b/CD18 rece

IL-8 expressionPMN chemotaxis

IL-8

Normal

UROPLAKIN

Pathogenesis of infection

Host factors – Distribution of receptors – carbohydrates –related to blood group carbohydrates

Immune response – Overactive –lots of PMN’sExcessive inflammation

Related to polymorphisms in specific Toll like receptorsGenetic predisposition

Microbial Factors

Presence of appropriate ligands- flagellaPathogenicity islands – groups of virulence-associatedgenes

How do E.coli become pathogenic in the gut ?

Acquisition of virulence genes:

From other E.coli/Shigella -

pili - Required to attach(different pili for each type of disease)

- bundle forming pili-cfa - colonization factor antigen

FECAL – ORAL contamination !

E.coli and diarrheal disease

Acquisition of virulence genes: TOXINS

ETEC - Toxigenic - secretory diarrhea – Traveler’sdiarrhea

EHEC - enterohemorrhagic - 0H157:H7 - toxigenic –

(Shiga toxin) – Hemolytic uremic syndromeInteracts with plateletsRenal endothelial cells(Jack in the Box hamburgers)

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Enteropathogenic E.coli “pink” = gram negative rodM. Donnenberg, Univ. Maryland

Enteropathogenic E.coli

Acquire the genes for virulence

Pathogenicity islandLigand to attach + toxin

Bundle forming pilus

Pedestal formation - attaching/effacing lesionLEE Locus -Type III secretion genes SYRINGE GENES

Intimin expression - adhesinTir - bacterially encoded receptor

.

Enteropathogenic E. coli

Activate rearrangements of the actin cytoskeleton

Stimulate phosphorylation of specific substrates

Interferes with the normal barrier function of the gutmucosal cell

E. coli - bundleforming pilus !

EnteropathogenicE.coli

Pedestal -attaching/effacing lesion

Locus of Enterocyte Effacement (LEE) pathogenicity island41 open reading framesnecessary and sufficient for attaching and effacing lesions

Genes - dark blue - esc genes- Yersinia type III secretion homologues

light blue - sep genes type III secretion system components

red encode the outer membrane adhesin intimin and its receptor Tir

teal blue - encode chaperones of secreted proteins

green encode -esp secreted proteins

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Enteropathogenic E.coli

Scanning EM - EPEC

ETEC

Toxigenic E.coli - like cholera -

Attachment - cfa pilus

Toxin - ADP ribosylating enzyme

ADP-ribose transferred to GTP bindingprotein of adenyl cyclase

Cl- secretion Na+ absorption

Secretory diarrhea

Enterohaemorrhagic E.coli

Pilin mediated attachmentPedestal formation – type III secretion+ cytoxin

HUS - small blood vessel damage affects glomeruliplateletsrenal failure

E.coli in the bloodstream - (perforated viscus etc)

LPS - endotoxin - actively shed

TLR4

CD14 + LBP

Toll like receptors and adaptor proteins

NF-kB activation

Macrophage or T cell (epithelial cells also)

SEPSIS

Lipopolysaccharide = Endotoxin

Gram negative bacteria – activate immune cells

“toxicity” varies with species – MICROBIAL FACTORS

Clinical severity – dependent upon the HOST response

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LPS

Peptidoglycan

Cytoplasmic

membrane

E.coli sepsis - organism in a normally sterile

Rapidly cleared - no immune response

Large inoculum - Activation of host cytokine expression

How are gram negative bacteria cleared from the blood ?

Innate immune defenses -“serum sensitive” - lysed by complementopsonized - phagocytosed

reticuloendothelial clearance mechanisms

P.aeruginosa

Opportunistic pathogen –

Causes disease in impaired hosts

Opportunistic pathogens

Pseudomonas aeruginosaGenetically versatile bacteriaFew growth requirementsRarely pathogenic in the normal host

Major pathogens in immunocompromisedpatientsSpecial settings - cystic fibrosis

Genomic sequencing – compare genetic organizationof pathogens and non-pathogens

Nature (2000) 406:959-964

http://www.pseudomonas.com

P. aeruginosagenome

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Virulence factors:

1- Turn on one group of genes in response to the environ-ment to ESTABLISH an infection

Flagella -motilityimmune activation

Hemolysins - Phospholipases - cleave host components

Proteases -

Siderophores - pigments - scavenge iron

Airway inflammationin the CF lung

PMN’s

Mucin

Bacteria

NeutrophilInflux and

Mucus Hypersecretion

Flagella -

Motility - swim toward a desired carbohydrateLigands - for mucins

clearance

Ligand for macrophages -

PA1244 - wild type DB103 – mutant – lacks flagella

Analysis of these pathways – Identify mutants

FlagellaMultiple interactions with the host

Highly immunostimulatoryMUCIN

NF-kB IL-8

Recruits and activates PMN’s

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How are flagella signaled ??

Tissue dependent – Organism dependent

Extracellular pathogen – Pseudomonas aeruginosaInhaled organismairway epithelial cells

TLR -5 (toll like receptors)

Flagella

TLR5

Merge

Human airway cells

Airway – superficial stimulus is sufficient to activate inflammationApical display of the toll like receptors

Mutations in TLR’s – associated with increased susceptibilityto specific bacterial infections

Intracellular pathogenSalmonella enteriditis

Gut pathogen – Need INVASION to activate inflammation

Flagella Ipaf IL-1

IL-18Monomeric flagellin – interacts with intracellular receptors

Mutations in these receptors – Inflammatory bowel disease

Two-component signaling cascades

Insures the expression of the multiple virulence genesappropriate for the environment

MotilityPiliMetabolic activation for growth

Pathogenicity island - often geographically linkedfacilitates transmission

Two component signaling -

Coordinate regulation of virulence genes

In response to a given environmental signal:

P

A B C

SENSORTranscription

Bacterial Adaptation –

Selection in vivo for “mutants” able to persist in thelung –

Less virulent – less “immunogenic”

don’t make flagella (ligand for macrophages)flagella stimulate PMN’s

Actively express groups of genes to facilitate persistencewithin the host:

(iron scavenging, immune evasion)

Communities - Biofilms

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Quorum sensing systems

• Coordinate expression of virulence factors -• Regulation via transcriptional activation

• Secretion of small diffusable molecules -organize the bacterial population to respond

• Biofilm production - SLIME

Quorum sensing -How do communities of bacteria coordinate theiractivities?

Examples - Biofilms - dental plaqueAirway colonizationInfected intravenous catheters

Acyl homoserine lactones - small highly diffusable molecules(gram negatives), others in gram positive organisms

HSL

HSL

HSL

HSL

HSL concentration is high - diffuses back into the bacteria

A B C

HSL

Transcriptional activation

Regulates the transcription of the same group of genes in manyorganisms at the same time – slime genes for example

Summary – Bacterial pathogenesis

Commensal flora –

Pathogens – acquire blocks of DNA – contribute to virulence

Microbial factors – adhesinstoxins

Host factors – Receptors – Tissue specificImmune responses

Opportunists –Adapt to the environmentGenetic flexibility – selection of mutants in vivoPersist -